HUE034777T2 - Monoclonal Antibodies Against Klaudin-18 To Treat Cancer - Google Patents
Monoclonal Antibodies Against Klaudin-18 To Treat Cancer Download PDFInfo
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- HUE034777T2 HUE034777T2 HUE10011776A HUE10011776A HUE034777T2 HU E034777 T2 HUE034777 T2 HU E034777T2 HU E10011776 A HUE10011776 A HU E10011776A HU E10011776 A HUE10011776 A HU E10011776A HU E034777 T2 HUE034777 T2 HU E034777T2
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Applications Claiming Priority (1)
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EP05025657A EP1790664A1 (en) | 2005-11-24 | 2005-11-24 | Monoclonal antibodies against claudin-18 for treatment of cancer |
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HUE034777T2 true HUE034777T2 (en) | 2018-02-28 |
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HUE10011772A HUE041538T2 (hu) | 2005-11-24 | 2006-11-24 | A claudin-18 elleni monoklonális antitestek a rák kezelésére |
HUE19202848A HUE058814T2 (hu) | 2005-11-24 | 2006-11-24 | Monoklonális antitestek a Claudin-18 ellen a rák kezelésére |
HUE10011776A HUE034777T2 (en) | 2005-11-24 | 2006-11-24 | Monoclonal Antibodies Against Klaudin-18 To Treat Cancer |
HUE10011775A HUE025578T2 (en) | 2005-11-24 | 2006-11-24 | Monoclonal Antibodies Against Klaudin-18 To Treat Cancer |
HUE10011773A HUE025900T2 (en) | 2005-11-24 | 2006-11-24 | Monoclonal Antibodies Against Klaudin-18 To Treat Cancer |
HUE17192466A HUE048404T2 (hu) | 2005-11-24 | 2006-11-24 | Claudin-18 elleni monoklonális antitestek rák kezelésére |
HUE18185237A HUE058777T2 (hu) | 2005-11-24 | 2006-11-24 | Monoklonális antitestek a Claudin-18 ellen a rák kezelésére |
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HUE10011772A HUE041538T2 (hu) | 2005-11-24 | 2006-11-24 | A claudin-18 elleni monoklonális antitestek a rák kezelésére |
HUE19202848A HUE058814T2 (hu) | 2005-11-24 | 2006-11-24 | Monoklonális antitestek a Claudin-18 ellen a rák kezelésére |
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Application Number | Title | Priority Date | Filing Date |
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HUE10011775A HUE025578T2 (en) | 2005-11-24 | 2006-11-24 | Monoclonal Antibodies Against Klaudin-18 To Treat Cancer |
HUE10011773A HUE025900T2 (en) | 2005-11-24 | 2006-11-24 | Monoclonal Antibodies Against Klaudin-18 To Treat Cancer |
HUE17192466A HUE048404T2 (hu) | 2005-11-24 | 2006-11-24 | Claudin-18 elleni monoklonális antitestek rák kezelésére |
HUE18185237A HUE058777T2 (hu) | 2005-11-24 | 2006-11-24 | Monoklonális antitestek a Claudin-18 ellen a rák kezelésére |
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JP (4) | JP5933157B2 (pt) |
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CN (3) | CN103509110B (pt) |
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BR (1) | BRPI0618920B8 (pt) |
CA (3) | CA2628126C (pt) |
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DK (8) | DK3421498T3 (pt) |
ES (8) | ES2407819T3 (pt) |
HK (5) | HK1119721A1 (pt) |
HR (8) | HRP20220246T3 (pt) |
HU (7) | HUE041538T2 (pt) |
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PL (8) | PL2325210T3 (pt) |
PT (8) | PT1948693E (pt) |
RS (8) | RS62886B1 (pt) |
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SG (2) | SG10201903351SA (pt) |
SI (8) | SI2311878T1 (pt) |
WO (1) | WO2007059997A1 (pt) |
Families Citing this family (125)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE10254601A1 (de) * | 2002-11-22 | 2004-06-03 | Ganymed Pharmaceuticals Ag | Differentiell in Tumoren exprimierte Genprodukte und deren Verwendung |
DE102004024617A1 (de) | 2004-05-18 | 2005-12-29 | Ganymed Pharmaceuticals Ag | Differentiell in Tumoren exprimierte Genprodukte und deren Verwendung |
WO2005121338A1 (ja) * | 2004-06-07 | 2005-12-22 | Kyowa Hakko Kogyo Co., Ltd. | 抗perp抗体 |
EP1790664A1 (en) | 2005-11-24 | 2007-05-30 | Ganymed Pharmaceuticals AG | Monoclonal antibodies against claudin-18 for treatment of cancer |
US8093362B2 (en) * | 2005-12-06 | 2012-01-10 | Kyowa Hakko Kirin Co., Ltd. | Anti-PERP recombinant antibody |
EP1997832A1 (en) * | 2007-05-29 | 2008-12-03 | Ganymed Pharmaceuticals AG | Monoclonal antibodies against Claudin-18 for treatment of cancer |
US20090123946A1 (en) * | 2007-10-19 | 2009-05-14 | Abbott Laboratories | Immunoassays and kits for the detection of ngal |
US8846036B2 (en) * | 2007-10-19 | 2014-09-30 | Abbott Laboratories | Antibodies that bind to mammalian NGAL and uses thereof |
US20090124022A1 (en) * | 2007-10-19 | 2009-05-14 | Abbott Laboratories | Antibodies that bind to mammalian ngal and uses thereof |
HUE064745T2 (hu) | 2009-02-20 | 2024-04-28 | Astellas Pharma Inc | Módszerek és készítmények a rák diagnosztizálására és kezelésére |
NZ734307A (en) * | 2009-11-11 | 2020-05-29 | Ganymed Pharmaceuticals Ag | Antibodies specific for claudin 6 (cldn6) |
PT2504363T (pt) * | 2009-11-24 | 2019-08-02 | Nat Res Council Canada | Anticorpos anticlusterina e fragmentos de ligação ao antigénio e a sua utilização para reduzir o volume de um tumor |
RU2740479C2 (ru) | 2010-02-24 | 2021-01-14 | Иммьюноджен, Инк. | Антитела против рецептора фолиевой кислоты 1, их иммуноконъюгаты и использование |
EP2404936A1 (en) * | 2010-07-06 | 2012-01-11 | Ganymed Pharmaceuticals AG | Cancer therapy using CLDN6 target-directed antibodies in vivo |
CA2813796C (en) * | 2010-10-18 | 2019-01-15 | Mediapharma S.R.L. | Erbb3 binding antibody |
EP3252076B1 (en) | 2011-01-14 | 2019-09-04 | The Regents Of The University Of California | Diagnostic use of antibodies against ror-1 protein |
EP3763740A1 (en) | 2011-01-26 | 2021-01-13 | Celldex Therapeutics, Inc. | Anti-kit antibodies and uses thereof |
CA2826563C (en) * | 2011-02-07 | 2020-10-20 | Paul Kussie | Methods and systems for treating eclampsia and pre-eclampsia |
US8722044B2 (en) | 2011-03-15 | 2014-05-13 | Janssen Biotech, Inc. | Human tissue factor antibody and uses thereof |
AU2012236219B2 (en) | 2011-04-01 | 2017-02-23 | Immunogen, Inc. | Methods for increasing efficacy of FOLR1 cancer therapy |
EP3026064B1 (en) * | 2011-05-13 | 2018-10-17 | Ganymed Pharmaceuticals GmbH | Antibodies for treatment of cancer expressing claudin 6 |
NZ626269A (en) * | 2011-12-20 | 2016-06-24 | Janssen Biotech Inc | Anti-phf-tau antibodies and their uses |
US9822170B2 (en) | 2012-02-22 | 2017-11-21 | Alethia Biotherapeutics Inc. | Co-use of a clusterin inhibitor with an EGFR inhibitor to treat cancer |
WO2013167153A1 (en) * | 2012-05-09 | 2013-11-14 | Ganymed Pharmaceuticals Ag | Antibodies useful in cancer diagnosis |
EP3254695B1 (en) | 2012-05-23 | 2020-09-09 | Astellas Pharma Inc. | Combination therapy involving antibodies against claudin 18.2 for treatment of cancer |
EP2852409B1 (en) | 2012-05-23 | 2020-03-25 | Astellas Pharma Inc. | Combination therapy involving antibodies against claudin 18.2 for treatment of cancer |
WO2013174404A1 (en) * | 2012-05-23 | 2013-11-28 | Ganymed Pharmaceuticals Ag | Combination therapy involving antibodies against claudin 18.2 for treatment of cancer |
WO2013174403A1 (en) * | 2012-05-23 | 2013-11-28 | Ganymed Pharmaceuticals Ag | Combination therapy involving antibodies against claudin 18.2 for treatment of cancer |
BR112015001459B1 (pt) | 2012-07-25 | 2023-02-14 | Celldex Therapeutics, Inc | Anticorpo isolado ou fragmento do mesmo, conjugado, usos dos mesmos, composição farmacêutica, polinucleotídeo, vetor, célula hospedeira, célula isolada, kit, método in vitro para inibir atividade da kit, método para produzir um anticorpo |
KR20200079565A (ko) | 2012-08-31 | 2020-07-03 | 이뮤노젠 아이엔씨 | 엽산 수용체 1의 검출을 위한 진단성 검정 및 키트 |
EP3766903A3 (en) * | 2012-11-13 | 2021-02-17 | BioNTech SE | Bispecific anti claudin xcd3 antibodies for treatment of claudin expressing cancer diseases |
RU2678127C2 (ru) * | 2012-11-13 | 2019-01-23 | Бионтех Аг | Агенты для лечения экспрессирующих клаудин раковых заболеваний |
CA2895508A1 (en) | 2012-12-18 | 2014-06-26 | Icahn School Of Medicine At Mount Sinai | Influenza virus vaccines and uses thereof |
WO2014127785A1 (en) * | 2013-02-20 | 2014-08-28 | Ganymed Pharmaceuticals Ag | Combination therapy involving antibodies against claudin 18.2 for treatment of cancer |
EP4177273A1 (en) * | 2013-02-20 | 2023-05-10 | Astellas Pharma Inc. | Combination therapy involving antibodies against claudin 18.2 for treatment of cancer |
WO2014159960A1 (en) | 2013-03-14 | 2014-10-02 | Icahn School Of Medicine At Mount Sinai | Antibodies against influenza virus hemagglutinin and uses thereof |
WO2014159531A1 (en) * | 2013-03-14 | 2014-10-02 | The Board Of Regents Of The University Of Texas System | Monoclonal antibodies targeting epcam for detection of prostate cancer lymph node metastases |
WO2014146672A1 (en) * | 2013-03-18 | 2014-09-25 | Ganymed Pharmaceuticals Ag | Therapy involving antibodies against claudin 18.2 for treatment of cancer |
EP2976360B1 (en) * | 2013-03-18 | 2019-11-27 | Astellas Pharma Inc. | Therapy involving antibodies against claudin 18.2 for treatment of cancer |
WO2015014376A1 (en) | 2013-07-31 | 2015-02-05 | Biontech Ag | Diagnosis and therapy of cancer involving cancer stem cells |
SG10201907501QA (en) | 2013-08-30 | 2019-10-30 | Immunogen Inc | Antibodies and assays for detection of folate receptor 1 |
AU2014346792A1 (en) | 2013-11-06 | 2016-06-02 | Abbvie Stemcentrx Llc | Novel anti-claudin antibodies and methods of use |
WO2015179737A2 (en) | 2014-05-23 | 2015-11-26 | Kolltan Pharmaceuticals, Inc. | Treatment of eosinophil or mast cell related disorders |
EP3851111A1 (en) * | 2014-07-10 | 2021-07-21 | Biothera, Inc. | Beta-glucan in combination with anti-cancer agents affecting the tumor microenvironment |
CN112979828A (zh) * | 2014-07-17 | 2021-06-18 | 恺兴生命科技(上海)有限公司 | 靶向cld18a2的t淋巴细胞及其制备方法和应用 |
EP3247389A4 (en) | 2015-01-23 | 2019-10-30 | Icahn School of Medicine at Mount Sinai | INFLUENZAVIRUSSCHUTZIMPFPLÄNE |
WO2016180468A1 (en) * | 2015-05-11 | 2016-11-17 | Biontech Cell & Gene Therapies Gmbh | Claudin-18.2-specific immunoreceptors and t cell epitopes |
SG11201710639YA (en) | 2015-06-22 | 2018-01-30 | Bayer Pharma AG | Antibody drug conjugates (adcs) and antibody prodrug conjugates (apdcs) with enzymatically cleavable groups |
JP6768011B2 (ja) * | 2015-06-23 | 2020-10-14 | バイエル ファーマ アクチエンゲゼルシャフト | キネシンスピンドルタンパク質(ksp)阻害剤の抗cd123抗体との抗体薬物複合体 |
US20190183930A1 (en) * | 2015-08-25 | 2019-06-20 | The Uab Research Foundation | Methods for stem cell transplantation |
US10172875B2 (en) | 2015-09-17 | 2019-01-08 | Immunogen, Inc. | Therapeutic combinations comprising anti-FOLR1 immunoconjugates |
EP3471767A4 (en) | 2016-06-15 | 2020-01-15 | Icahn School of Medicine at Mount Sinai | INFLUENZA VIRUS HEMAGGLUTININS AND USES THEREOF |
EP3919518A1 (en) | 2016-06-15 | 2021-12-08 | Bayer Pharma Aktiengesellschaft | Specific antibody-drug-conjugates (adcs) with ksp inhibitors and anti-cd123-antibodies |
JP2019517813A (ja) * | 2016-06-16 | 2019-06-27 | ザ ボード オブ トラスティーズ オブ ザ レランド スタンフォード ジュニア ユニバーシティー | Cd81に対するヒト化及びキメラモノクローナル抗体 |
WO2018006882A1 (zh) * | 2016-07-08 | 2018-01-11 | 科济生物医药(上海)有限公司 | 抗密蛋白18a2的抗体及其应用 |
WO2018114578A1 (de) | 2016-12-21 | 2018-06-28 | Bayer Pharma Aktiengesellschaft | Binder-wirkstoff-konjugate (adcs) mit enzymatisch spaltbaren gruppen |
CA3047522A1 (en) | 2016-12-21 | 2018-06-28 | Bayer Pharma Aktiengesellschaft | Specific antibody drug conjugates (adcs) having ksp inhibitors |
JOP20180021A1 (ar) | 2017-03-16 | 2019-01-30 | Janssen Biotech Inc | الأجسام المضادة لتكتلات خيوط بروتين تاو (tau) الحلزونية المزدوجة واستخداماتها |
CA3058652A1 (en) | 2017-04-07 | 2018-10-11 | Icahn School Of Medicine At Mount Sinai | Anti-influenza b virus neuraminidase antibodies and uses thereof |
SG11202007055QA (en) * | 2018-03-08 | 2020-09-29 | Phanes Therapeutics Inc | Anti-claudin 18.2 antibodies and uses thereof |
AU2019232759A1 (en) * | 2018-03-08 | 2020-08-27 | Phanes Therapeutics, Inc. | Anti-TIP-1 antibodies and uses thereof |
WO2019170147A1 (zh) | 2018-03-09 | 2019-09-12 | 科济生物医药(上海)有限公司 | 用于治疗肿瘤的方法和组合物 |
KR102340989B1 (ko) | 2018-03-28 | 2021-12-20 | 에이비온 주식회사 | 클라우딘 3의 ecl-2에 특이적으로 결합하는 항체, 이의 단편 및 이들의 용도 |
CN108517315B (zh) * | 2018-03-30 | 2019-06-04 | 四川迈克生物新材料技术有限公司 | 抗人IgM单克隆抗体、其杂交瘤细胞株及应用 |
EP3794037A4 (en) | 2018-05-18 | 2022-03-02 | Lanova Medicines Limited Company | ANTI-CLAUDIN 18.2 ANTIBODIES AND USES THEREOF |
CN112513093B (zh) * | 2018-07-18 | 2024-08-09 | 奥美药业有限公司 | 一种新型抗体及其制备方法和应用 |
WO2020023548A1 (en) * | 2018-07-23 | 2020-01-30 | Abexxa Biologics, Inc. | Antibodies targeting a complex comprising non-classical hla-i and neoantigen and their methods of use |
KR20210050547A (ko) | 2018-08-27 | 2021-05-07 | 난징 산홈 팔마세우티칼 컴퍼니 리미티드 | 항-클라우딘18.2 항체 및 이의 용도 |
US20210403552A1 (en) | 2018-10-22 | 2021-12-30 | Shanghai GenBase Biotechnology Co., Ltd. | Anti-cldn18.2 antibody and uses thereof |
JP7458399B2 (ja) * | 2018-12-07 | 2024-03-29 | ゼットリップ ホールディング リミテッド | 抗クローディン抗体及びそれらの使用 |
CA3125193A1 (en) * | 2018-12-28 | 2020-07-02 | Nanjing GenScript Biotech Co., Ltd. | Claudin18.2 binding moieties and uses thereof |
US20230192840A1 (en) | 2018-12-28 | 2023-06-22 | Sichuan Kelun-Biotech Biopharmaceutical Co., Ltd. | Antibody and use thereof |
CN113227135A (zh) * | 2018-12-28 | 2021-08-06 | 斯帕克斯治疗公司 | 用于治疗癌症和其他疾病的对紧密连接蛋白18.2具有特异性的结合分子、其组合物和方法 |
CN111434692B (zh) * | 2019-01-15 | 2021-12-31 | 浙江道尔生物科技有限公司 | 抗cld18a2纳米抗体及其应用 |
CN109762067B (zh) * | 2019-01-17 | 2020-02-28 | 北京天广实生物技术股份有限公司 | 结合人Claudin 18.2的抗体及其用途 |
AU2020217012A1 (en) | 2019-02-01 | 2021-08-19 | Novarock Biotherapeutics, Ltd. | Anti-claudin 18 antibodies and methods of use thereof |
US20220153873A1 (en) * | 2019-04-24 | 2022-05-19 | Icahn School Of Medicine At Mount Sinai | Anti-influenza b virus neuraminidase antibodies and uses thereof |
MX2021013532A (es) | 2019-05-08 | 2022-02-11 | Janssen Biotech Inc | Materiales y metodos para modular la inmunidad mediada por celulas t. |
CN117264059A (zh) * | 2019-05-16 | 2023-12-22 | 启愈生物技术(上海)有限公司 | 抗cldn抗体及其药物组合物和检测方法 |
KR20220024010A (ko) | 2019-05-16 | 2022-03-03 | 치루 파머수티컬 컴퍼니 리미티드 | 클라우딘 18a2에 대한 항체 및 그의 용도 |
TW202108627A (zh) * | 2019-05-24 | 2021-03-01 | 大陸商三優生物醫藥(上海)有限公司 | 新型cldn18.2結合分子 |
US20220306765A1 (en) * | 2019-08-20 | 2022-09-29 | Suzhou Transcenta Therapeutics Co., Ltd. | Novel anti-cldn18.2 antibodies |
CN119019558A (zh) | 2019-08-22 | 2024-11-26 | 浙江道尔生物科技有限公司 | 抗pd-l1纳米抗体 |
CN112574307B (zh) * | 2019-09-29 | 2023-11-28 | 迈威(上海)生物科技股份有限公司 | 抗人Claudin18.2抗体及其应用 |
CN112707965A (zh) * | 2019-09-30 | 2021-04-27 | 和铂医药(苏州)有限公司 | 靶向cldn18.2的抗体及其制备方法和应用 |
PE20221459A1 (es) * | 2019-11-05 | 2022-09-21 | Lanova Medicines Ltd | Conjugados anticuerpo-farmaco dirigido a claudina 18.2 |
JP2023505318A (ja) | 2019-12-06 | 2023-02-08 | ソティオ バイオテック エイ.エス. | ヒト化cldn18.2抗体 |
WO2021119508A1 (en) * | 2019-12-13 | 2021-06-17 | Alector Llc | Anti-mertk antibodies and methods of use thereof |
EP4081307A1 (en) * | 2019-12-23 | 2022-11-02 | SOTIO Biotech a.s. | Tumor-specific claudin 18.2 antibodies |
IL294218A (en) * | 2019-12-27 | 2022-08-01 | Chiome Bioscience Inc | Anti-cdcp1 antibody |
CN116096751A (zh) * | 2020-02-25 | 2023-05-09 | 璟尚生物制药公司 | 三特异性t细胞接合器 |
AU2021225870A1 (en) * | 2020-02-27 | 2022-10-20 | Janssen Biotech, Inc. | Materials and methods for modulating an immune response |
CN115397856A (zh) | 2020-03-30 | 2022-11-25 | 生物技术公司 | 靶向密蛋白-18.2的rna组合物 |
CN113493515B (zh) * | 2020-04-02 | 2023-03-28 | 广东菲鹏制药股份有限公司 | 抗cldn18a2的抗体以及治疗肿瘤的药物 |
WO2021228141A1 (zh) * | 2020-05-15 | 2021-11-18 | 四川科伦博泰生物医药股份有限公司 | 抗体药物缀合物及其制备方法和用途 |
TW202212360A (zh) * | 2020-05-25 | 2022-04-01 | 中國大陸商蘇州創勝醫藥集團有限公司 | 抗cldn18.2抗體及其診斷用途 |
WO2021239026A1 (zh) * | 2020-05-29 | 2021-12-02 | 杭州邦顺制药有限公司 | 针对Claudin18.2的抗体及其用途 |
US10981996B1 (en) | 2020-06-01 | 2021-04-20 | Abexxa Biologics, Inc. | Antibodies targeting a complex comprising non-classical HLA-I and neoantigen and their methods of use |
US10981997B1 (en) | 2020-06-01 | 2021-04-20 | Abexxa Biologics, Inc. | Antibodies targeting a complex comprising non-classical HLA-I and neoantigen and their methods of use |
US11976120B2 (en) | 2020-06-01 | 2024-05-07 | Boehringer Ingelheim International Gmbh | Antibodies targeting a complex comprising non-classical HLA-I and neoantigen and their methods of use |
CN113754778A (zh) * | 2020-06-05 | 2021-12-07 | 上海交通大学 | 靶向cldn18.2的嵌合抗原受体及其用途 |
CN111777681B (zh) * | 2020-07-06 | 2022-10-11 | 康诺亚生物医药科技(成都)有限公司 | 一种结合紧密连接蛋白-18.2的抗体及其用途 |
CN113929780A (zh) * | 2020-07-13 | 2022-01-14 | 北京凯因科技股份有限公司 | 一种结合密蛋白的用于治疗癌症的人源化抗体 |
BR112023000657A2 (pt) | 2020-07-13 | 2023-01-31 | Shanghai Junshi Biosciences Co Ltd | Anticorpo anti-cldn-18.2 e uso do mesmo |
WO2022011531A1 (zh) * | 2020-07-14 | 2022-01-20 | 浙江道尔生物科技有限公司 | 一种抗cld18a2的单域抗体 |
AU2021345124A1 (en) | 2020-09-16 | 2023-03-30 | Amgen Inc. | Methods for administering therapeutic doses of bispecific T-cell engaging molecules for the treatment of cancer |
CN114316046B (zh) * | 2020-09-29 | 2024-08-09 | 北京凯因科技股份有限公司 | 一种稳定的抗体组合物 |
AU2021372463A1 (en) | 2020-10-28 | 2023-06-22 | Janssen Biotech, Inc. | Compositions and methods for modulating delta gamma chain mediated immunity |
JP2023548538A (ja) | 2020-11-08 | 2023-11-17 | シージェン インコーポレイテッド | 併用療法 |
CN112480248B (zh) | 2020-11-24 | 2023-05-05 | 三优生物医药(上海)有限公司 | 与cld18a2特异性结合的分子 |
WO2022122709A1 (en) | 2020-12-07 | 2022-06-16 | Sotio Biotech A.S. | Antibody-drug conjugates based on humanized cldn18.2 antibodies |
IL302894A (en) | 2020-12-23 | 2023-07-01 | Sotio Biotech A S | Tumor-specific claudin 18.2 antibody-drug conjugates |
CN114685660A (zh) | 2020-12-30 | 2022-07-01 | 百奥泰生物制药股份有限公司 | 抗cldn18.2抗体及其制备方法和应用 |
AU2022223150A1 (en) * | 2021-02-19 | 2023-09-21 | Beijing Cancer Hospital | Anti-cldn18.2 antibody conjugates |
CN117083299A (zh) | 2021-04-02 | 2023-11-17 | 原启生物科技(上海)有限责任公司 | Cldn18.2抗原结合蛋白及其用途 |
WO2022226079A1 (en) * | 2021-04-20 | 2022-10-27 | Inbios International, Inc. | Neutralizing antibodies against sars-cov-2 |
JP2024520674A (ja) | 2021-06-02 | 2024-05-24 | バイオ-テラ ソリュ-ションズ,エルティーディー. | 薬物コンジュゲート及びその使用 |
WO2022262959A1 (en) | 2021-06-15 | 2022-12-22 | Astellas Pharma Europe Bv | Bispecific binding agents binding to cldn18.2 and cd3 |
EP4355784A1 (en) | 2021-06-15 | 2024-04-24 | Xencor, Inc. | Heterodimeric antibodies that bind claudin18.2 and cd3 |
AU2022325498A1 (en) | 2021-08-13 | 2024-02-01 | Cytune Pharma | Il-2/il-15rbetagamma agonist combination with antibody-drug conjugates for treating cancer |
AU2022350588A1 (en) | 2021-09-27 | 2024-05-02 | Evopoint Biosciences Co., Ltd. | Antibody, antibody-drug conjugate thereof and use thereof |
EP4482859A1 (en) | 2022-02-27 | 2025-01-01 | Boehringer Ingelheim International GmbH | Bispecific antibodies against cd277 and a tumor-antigen |
WO2024074634A1 (en) | 2022-10-06 | 2024-04-11 | BioNTech SE | Rna compositions targeting claudin-18.2 |
WO2024074211A1 (en) | 2022-10-06 | 2024-04-11 | BioNTech SE | Rna compositions targeting claudin-18.2 |
CN115819586B (zh) * | 2022-10-13 | 2023-10-31 | 珠海市丽珠单抗生物技术有限公司 | 抗人SIRPα单克隆抗体及其用途 |
Family Cites Families (205)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3044382A (en) | 1957-12-14 | 1962-07-17 | Compur Werk Friedrich Deckel | Photographic shutter |
US4475196A (en) | 1981-03-06 | 1984-10-02 | Zor Clair G | Instrument for locating faults in aircraft passenger reading light and attendant call control system |
US4447233A (en) | 1981-04-10 | 1984-05-08 | Parker-Hannifin Corporation | Medication infusion pump |
US4474893A (en) | 1981-07-01 | 1984-10-02 | The University of Texas System Cancer Center | Recombinant monoclonal antibodies |
US4439196A (en) | 1982-03-18 | 1984-03-27 | Merck & Co., Inc. | Osmotic drug delivery system |
US4522811A (en) | 1982-07-08 | 1985-06-11 | Syntex (U.S.A.) Inc. | Serial injection of muramyldipeptides and liposomes enhances the anti-infective activity of muramyldipeptides |
US4447224A (en) | 1982-09-20 | 1984-05-08 | Infusaid Corporation | Variable flow implantable infusion apparatus |
US4487603A (en) | 1982-11-26 | 1984-12-11 | Cordis Corporation | Implantable microinfusion pump system |
US4486194A (en) | 1983-06-08 | 1984-12-04 | James Ferrara | Therapeutic device for administering medicaments through the skin |
US4596556A (en) | 1985-03-25 | 1986-06-24 | Bioject, Inc. | Hypodermic injection apparatus |
US5374548A (en) | 1986-05-02 | 1994-12-20 | Genentech, Inc. | Methods and compositions for the attachment of proteins to liposomes using a glycophospholipid anchor |
MX9203291A (es) | 1985-06-26 | 1992-08-01 | Liposome Co Inc | Metodo para acoplamiento de liposomas. |
GB8601597D0 (en) | 1986-01-23 | 1986-02-26 | Wilson R H | Nucleotide sequences |
US4954617A (en) | 1986-07-07 | 1990-09-04 | Trustees Of Dartmouth College | Monoclonal antibodies to FC receptors for immunoglobulin G on human mononuclear phagocytes |
US5260203A (en) | 1986-09-02 | 1993-11-09 | Enzon, Inc. | Single polypeptide chain binding molecules |
US4881175A (en) | 1986-09-02 | 1989-11-14 | Genex Corporation | Computer based system and method for determining and displaying possible chemical structures for converting double- or multiple-chain polypeptides to single-chain polypeptides |
US4946778A (en) | 1987-09-21 | 1990-08-07 | Genex Corporation | Single polypeptide chain binding molecules |
WO1988007089A1 (en) | 1987-03-18 | 1988-09-22 | Medical Research Council | Altered antibodies |
US5013653A (en) | 1987-03-20 | 1991-05-07 | Creative Biomolecules, Inc. | Product and process for introduction of a hinge region into a fusion protein to facilitate cleavage |
DE3853515T3 (de) | 1987-05-21 | 2005-08-25 | Micromet Ag | Multifunktionelle proteine mit vorbestimmter zielsetzung. |
US5258498A (en) | 1987-05-21 | 1993-11-02 | Creative Biomolecules, Inc. | Polypeptide linkers for production of biosynthetic proteins |
US5091513A (en) | 1987-05-21 | 1992-02-25 | Creative Biomolecules, Inc. | Biosynthetic antibody binding sites |
US5132405A (en) | 1987-05-21 | 1992-07-21 | Creative Biomolecules, Inc. | Biosynthetic antibody binding sites |
US4941880A (en) | 1987-06-19 | 1990-07-17 | Bioject, Inc. | Pre-filled ampule and non-invasive hypodermic injection device assembly |
US4790824A (en) | 1987-06-19 | 1988-12-13 | Bioject, Inc. | Non-invasive hypodermic injection device |
GB8717430D0 (en) | 1987-07-23 | 1987-08-26 | Celltech Ltd | Recombinant dna product |
GB8809129D0 (en) | 1988-04-18 | 1988-05-18 | Celltech Ltd | Recombinant dna methods vectors and host cells |
US5108921A (en) | 1989-04-03 | 1992-04-28 | Purdue Research Foundation | Method for enhanced transmembrane transport of exogenous molecules |
US6020145A (en) * | 1989-06-30 | 2000-02-01 | Bristol-Myers Squibb Company | Methods for determining the presence of carcinoma using the antigen binding region of monoclonal antibody BR96 |
US5312335A (en) | 1989-11-09 | 1994-05-17 | Bioject Inc. | Needleless hypodermic injection device |
US5064413A (en) | 1989-11-09 | 1991-11-12 | Bioject, Inc. | Needleless hypodermic injection device |
EP0507868A4 (en) | 1989-12-27 | 1992-11-04 | Us Commerce | Diagnostic probe for detecting human stomach cancer |
US6255458B1 (en) | 1990-08-29 | 2001-07-03 | Genpharm International | High affinity human antibodies and human antibodies against digoxin |
GB9019812D0 (en) | 1990-09-11 | 1990-10-24 | Scotgen Ltd | Novel antibodies for treatment and prevention of infection in animals and man |
US5383851A (en) | 1992-07-24 | 1995-01-24 | Bioject Inc. | Needleless hypodermic injection device |
GB9223377D0 (en) | 1992-11-04 | 1992-12-23 | Medarex Inc | Humanized antibodies to fc receptors for immunoglobulin on human mononuclear phagocytes |
US5589579A (en) | 1994-07-19 | 1996-12-31 | Cytoclonal Pharmaceutics, Inc. | Gene sequence and probe for a marker of non-small cell lung carinoma |
WO2000077037A2 (en) | 1999-06-15 | 2000-12-21 | Genentech, Inc. | Secreted and transmembrane polypeptides and nucleic acids encoding the same |
US6121022A (en) | 1995-04-14 | 2000-09-19 | Genentech, Inc. | Altered polypeptides with increased half-life |
US5677139A (en) | 1995-04-21 | 1997-10-14 | President And Fellows Of Harvard College | In vitro differentiation of CD34+ progenitor cells into T lymphocytes |
UA56132C2 (uk) | 1995-04-25 | 2003-05-15 | Смітклайн Бічем Байолоджікалс С.А. | Композиція вакцини (варіанти), спосіб стабілізації qs21 відносно гідролізу (варіанти), спосіб приготування композиції вакцини |
BR9707125A (pt) | 1996-01-11 | 1999-07-20 | Corixa Corp | Composições e processos para o tratamento e diagnóstico de câncer de mama |
WO2000075327A1 (en) | 1999-06-02 | 2000-12-14 | Genentech, Inc. | Methods and compositions for inhibiting neoplastic cell growth |
US6277375B1 (en) | 1997-03-03 | 2001-08-21 | Board Of Regents, The University Of Texas System | Immunoglobulin-like domains with increased half-lives |
US20070224663A1 (en) | 1997-03-07 | 2007-09-27 | Human Genome Sciences, Inc. | Human Secreted Proteins |
US7368531B2 (en) | 1997-03-07 | 2008-05-06 | Human Genome Sciences, Inc. | Human secreted proteins |
US7411051B2 (en) | 1997-03-07 | 2008-08-12 | Human Genome Sciences, Inc. | Antibodies to HDPPA04 polypeptide |
WO2000078961A1 (en) | 1999-06-23 | 2000-12-28 | Genentech, Inc. | Secreted and transmembrane polypeptides and nucleic acids encoding the same |
WO2000056889A2 (en) | 1999-03-23 | 2000-09-28 | Genentech, Inc. | Secreted and transmembrane polypeptides and nucleic acids encoding the same |
US20020127584A1 (en) | 1997-09-18 | 2002-09-12 | Genentech, Inc. | Secreted and transmembrane polypeptides and nucleic acids encoding the same |
US20030073129A1 (en) | 1998-09-01 | 2003-04-17 | Genentech, Inc. | Secreted and transmembrane polypeptides and nucleic acids encoding the same |
US20030022298A1 (en) | 1997-09-15 | 2003-01-30 | Genentech, Inc. | Secreted and transmembrane polypeptides and nucleic acids encoding the same |
US20030027272A1 (en) | 1997-09-18 | 2003-02-06 | Genentech, Inc. | Secreted and transmembrane polypeptides and nucleic acids encoding the same |
US20030170794A1 (en) | 1997-09-18 | 2003-09-11 | Genentech, Inc. | Secreted and transmembrane polypeptides and nucleic acids encoding the same |
US20030166104A1 (en) | 1997-09-18 | 2003-09-04 | Genentech, Inc. | Secreted and transmembrane polypeptides and nucleic acids encoding the same |
US20030008352A1 (en) | 1997-09-18 | 2003-01-09 | Genentech, Inc. | Secreted and transmembrane polypeptides and nucleic acids encoding the same |
US20050196832A1 (en) | 1997-09-18 | 2005-09-08 | Genentech, Inc. | Secreted and transmembrane polypeptides and nucleic acids encoding the same |
US7160985B2 (en) | 1997-10-29 | 2007-01-09 | Genentech, Inc. | Pro180 polypeptide |
US6194551B1 (en) | 1998-04-02 | 2001-02-27 | Genentech, Inc. | Polypeptide variants |
US20030022835A1 (en) | 1998-04-29 | 2003-01-30 | Genesis Research And Development Corporation Limited | Compositions isolated from skin cells and methods for their use |
US20030040471A1 (en) | 1998-04-29 | 2003-02-27 | Watson James D. | Compositions isolated from skin cells and methods for their use |
JP3428441B2 (ja) | 1998-05-15 | 2003-07-22 | エーザイ株式会社 | タイトジャンクション構成膜蛋白質クローディンファミリー |
US7319008B2 (en) | 1998-06-02 | 2008-01-15 | Genentech, Inc. | Nucleic acid underexpressed in melanoma |
US7351543B2 (en) | 1998-06-02 | 2008-04-01 | Genentech, Inc. | Antibodies to a polypeptide encoded by a nucleic acid underexpressed in melanoma |
JP2002517222A (ja) | 1998-06-11 | 2002-06-18 | スミスクライン ビーチャム コーポレーション | Gpr35a受容体 |
EP1104486A4 (en) | 1998-08-04 | 2002-07-17 | Diadexus Llc | NEW METHOD FOR DIAGNOSIS, FOLLOW-UP, AND IMAGE OF LUNG CANCER |
US20030166132A1 (en) | 1998-08-26 | 2003-09-04 | Genentech, Inc. | Secreted and transmembrane polypeptides and nucleic acids encoding the same |
US20030082626A1 (en) | 1998-09-01 | 2003-05-01 | Genentech, Inc. | Secreted and transmembrane polypeptides and nucleic acids encoding the same |
US20030187191A1 (en) | 1998-09-01 | 2003-10-02 | Genentech, Inc. | Secreted and transmembrane polypeptides and nucleic acids encoding the same |
US20050181478A1 (en) | 1998-09-01 | 2005-08-18 | Baker Kevin P. | Secreted and transmembrane polypeptides and nucleic acids encoding the same |
NZ531664A (en) | 1998-09-01 | 2005-07-29 | Genentech Inc | Pro1317 polypeptides and sequences thereof with homology to the semaphorin B glycoprotein family |
US20030054406A1 (en) | 1998-09-01 | 2003-03-20 | Genentech, Inc. | Secreted and transmembrane polypeptides and nucleic acids encoding the same |
CA2343577A1 (en) | 1998-09-16 | 2000-03-23 | Genentech, Inc. | Secreted and transmembrane polypeptides and nucleic acids encoding the same |
JP2002524103A (ja) | 1998-09-16 | 2002-08-06 | ザイモジェネティクス,インコーポレイティド | 胃ポリペプチドzsig28 |
WO2000020447A2 (en) | 1998-10-06 | 2000-04-13 | Curagen Corporation | Polynucleotides coding for secreted polypeptides, some having similarity to syncollin or claudin or cytokine, their therapeutic uses |
US7399834B2 (en) | 1998-10-07 | 2008-07-15 | Genentech, Inc. | Anti-PRO1558 antibodies |
EP1080209A2 (en) | 1998-10-21 | 2001-03-07 | Arch Development Corporation | Methods of treatment of type 2 diabetes |
US7026449B2 (en) | 1999-01-05 | 2006-04-11 | Genentech, Inc. | Secreted and transmembrane polypeptides and nucleic acids encoding the same |
KR20030002292A (ko) | 1999-03-08 | 2003-01-08 | 제넨테크, 인크. | 분비 및 막횡단 폴리펩티드 및 이를 코딩하는 핵산 |
US7109292B2 (en) | 1999-03-08 | 2006-09-19 | Genentech, Inc. | Secreted and transmembrane polypeptides and nucleic acids encoding the same |
US7507404B2 (en) | 1999-03-08 | 2009-03-24 | Genentech, Inc. | Secreted and transmembrane polypeptides and nucleic acids encoding the same |
EP1159419A1 (en) | 1999-03-08 | 2001-12-05 | Genentech, Inc. | Promotion or inhibition of angiogenesis and cardiovascularization |
JP2004507202A (ja) | 1999-03-31 | 2004-03-11 | キュラジェン コーポレイション | ポリペプチドをコードするオープンリーディングフレームを含む核酸;「orfx」 |
US20080286821A1 (en) | 1999-05-14 | 2008-11-20 | Eaton Dan L | Secreted and transmembrane polypeptides and nucleic acids encoding the same |
WO2003014303A2 (en) | 2001-08-03 | 2003-02-20 | Arbor Vita Corporation | Molecular interactions in cells |
AU2215300A (en) | 1999-06-02 | 2000-12-28 | Genentech Inc. | Methods and compositions for inhibiting neoplastic cell growth |
DK1185648T3 (da) | 1999-06-02 | 2007-07-30 | Genentech Inc | Fremgangsmåder og sammensætninger til inhibition af neoplastisk cellevækst |
AU3774300A (en) | 1999-06-02 | 2000-12-18 | Genentech Inc. | Secreted and transmembrane polypeptides and nucleic acids encoding the same |
AU2883900A (en) | 1999-07-07 | 2001-01-30 | Genentech Inc. | Secreted and transmembrane polypeptides and nucleic acids encoding the same |
US7754855B1 (en) * | 1999-07-13 | 2010-07-13 | Bolder Biotechnology, Inc. | Immunoglobulin fusion proteins |
EP1208202A2 (en) | 1999-09-01 | 2002-05-29 | Genentech, Inc. | Secreted and transmembrane polypeptides and nucleic acids encoding the same |
WO2001027257A1 (en) | 1999-10-14 | 2001-04-19 | The Board Of Trustees Of The University Of Arkansas | Tumor antigen derived gene-16 (tadg-16): a novel extracellular serine protease and uses thereof |
EP1250426A2 (en) | 1999-12-01 | 2002-10-23 | Genentech Inc. | Secreted and transmembrane polypeptides and nucleic acids encoding same |
US6380362B1 (en) | 1999-12-23 | 2002-04-30 | Genesis Research & Development Corporation Ltd. | Polynucleotides, polypeptides expressed by the polynucleotides and methods for their use |
CA2390685C (en) | 2000-01-06 | 2008-04-22 | Genentech, Inc. | Methods and compositions for inhibiting neoplastic cell growth |
EP1251863A4 (en) | 2000-01-31 | 2005-03-02 | Human Genome Sciences Inc | 22 SEPARATE HUMAN PROTEINS |
WO2001055326A2 (en) | 2000-01-31 | 2001-08-02 | Human Genome Sciences, Inc. | Nucleic acids, proteins, and antibodies |
CA2395178A1 (en) | 2000-01-31 | 2001-08-02 | Human Genome Sciences, Inc. | Nucleic acids, proteins, and antibodies |
US20040018969A1 (en) | 2000-01-31 | 2004-01-29 | Rosen Craig A. | Nucleic acids, proteins, and antibodies |
CA2401070A1 (en) | 2000-02-22 | 2001-08-30 | Corixa Corporation | Compositions and methods for diagnosis and therapy of malignant mesothelioma |
AU6802801A (en) | 2000-03-01 | 2001-09-24 | Genentech Inc | Secreted and transmembrane polypeptides and nucleic acids encoding the same |
WO2001070979A2 (en) | 2000-03-21 | 2001-09-27 | Millennium Pharmaceuticals, Inc. | Genes, compositions, kits, and method for identification, assessment, prevention and therapy of ovarian cancer |
US6436703B1 (en) | 2000-03-31 | 2002-08-20 | Hyseq, Inc. | Nucleic acids and polypeptides |
EP2067488A1 (en) | 2000-04-12 | 2009-06-10 | Human Genome Sciences, Inc. | Albumin fusion proteins |
WO2001090357A1 (en) | 2000-05-24 | 2001-11-29 | Genesis Research & Development Corporation Limited | Compositions isolated from skin cells and methods for their use |
CA2411828A1 (en) * | 2000-06-23 | 2002-01-03 | Maxygen, Inc. | Novel co-stimulatory molecules |
AU2001271589A1 (en) | 2000-06-30 | 2002-01-14 | Zymogenetics Inc. | Mammalian secreted proteins |
US7129084B2 (en) | 2000-08-03 | 2006-10-31 | Therapeutic Human Polyclonals, Inc. | Production of humanized antibodies in transgenic animals |
ES2284678T3 (es) | 2000-08-15 | 2007-11-16 | Immunex Corporation | Polipeptidos de claudinas. |
EP1309679A2 (en) | 2000-08-16 | 2003-05-14 | Chiron Corporation | Human genes and gene expression products |
US7442765B2 (en) | 2000-08-24 | 2008-10-28 | Genentech, Inc. | Secreted transmembrane polypeptides and nucleic acids encoding the same |
WO2002018576A2 (en) | 2000-08-28 | 2002-03-07 | Diadexus, Inc. | Compositions and methods relating to lung specific genes |
US7060800B2 (en) | 2000-09-08 | 2006-06-13 | Schering Corporation | Antibodies binding the TNF related protein, TNF-X |
AU2001292728A1 (en) | 2000-09-18 | 2002-03-26 | Thomas Jefferson University | Compositions and methods for identifying and targeting stomach and esophageal cancer cells |
AU3942202A (en) | 2000-11-30 | 2002-06-11 | Medarex Inc | Transgenic transchromosomal rodents for making human antibodies |
WO2002061087A2 (en) | 2000-12-19 | 2002-08-08 | Lifespan Biosciences, Inc. | Antigenic peptides, such as for g protein-coupled receptors (gpcrs), antibodies thereto, and systems for identifying such antigenic peptides |
AU2002255478A1 (en) | 2001-01-10 | 2002-09-12 | Pe Corporation (Ny) | Kits, such as nucleic acid arrays, comprising a majority of human exons or transcripts, for detecting expression and other uses thereof |
US7754208B2 (en) | 2001-01-17 | 2010-07-13 | Trubion Pharmaceuticals, Inc. | Binding domain-immunoglobulin fusion proteins |
US20030133939A1 (en) | 2001-01-17 | 2003-07-17 | Genecraft, Inc. | Binding domain-immunoglobulin fusion proteins |
CA2440008A1 (en) | 2001-01-29 | 2002-08-29 | Phase-1 Molecular Toxicology, Inc. | Rat toxicologically relevant genes and uses thereof |
CA2439383A1 (en) | 2001-02-26 | 2002-09-06 | Arena Pharmaceuticals, Inc. | Endogenous and non-endogenous versions of human g protein-coupled receptors |
US20030152939A1 (en) | 2001-04-09 | 2003-08-14 | Glennda Smithson | Novel secreted proteins and polynucleotides encoding them |
US20060084794A1 (en) | 2001-04-12 | 2006-04-20 | Human Genome Sciences, Inc. | Albumin fusion proteins |
JP2003000249A (ja) | 2001-05-10 | 2003-01-07 | Daiichi Fine Chemical Co Ltd | クローディンによるMT−MMPsを介したproMMP−2活性化 |
CA2449042A1 (en) | 2001-05-30 | 2002-12-27 | Biomedical Center | In silico screening for phenotype-associated expressed sequences |
EP1493028A4 (en) | 2001-07-06 | 2006-06-14 | Genentech Inc | PHAGEN DISPLAY PRESENTED LIGANDS OF THE PDZ DOMAIN |
US6551893B1 (en) | 2001-11-27 | 2003-04-22 | Micron Technology, Inc. | Atomic layer deposition of capacitor dielectric |
US20040002587A1 (en) | 2002-02-20 | 2004-01-01 | Watkins Jeffry D. | Fc region variants |
CA2379661A1 (en) | 2002-03-28 | 2003-09-28 | Kursad Turksen | Paracellular drug delivery system |
WO2003101283A2 (en) | 2002-06-04 | 2003-12-11 | Incyte Corporation | Diagnostics markers for lung cancer |
RU2005100777A (ru) * | 2002-06-14 | 2005-08-27 | Иммуномедикс, Инк. (Us) | Моноклональное антитело рам4 и его применение для диагностики и лечения рака поджелудочной железы |
EP2042517B1 (en) * | 2002-09-27 | 2012-11-14 | Xencor, Inc. | Optimized FC variants and methods for their generation |
SI1558648T1 (sl) | 2002-10-17 | 2012-05-31 | Genmab As | Človeška monoklonalna protitelesa proti CD |
EP1578365A4 (en) | 2002-11-14 | 2009-09-23 | Arbor Vita Corp | MOLECULAR INTERACTIONS IN NEURONS |
DE10254601A1 (de) * | 2002-11-22 | 2004-06-03 | Ganymed Pharmaceuticals Ag | Differentiell in Tumoren exprimierte Genprodukte und deren Verwendung |
EP1430902A1 (en) | 2002-12-20 | 2004-06-23 | Mondobiotech Laboratories Anstalt | Pharmaceutical composition of interferon gamma with molecular diagnostics for the improved treatment of asthma bronchiale |
WO2004063351A2 (en) | 2003-01-09 | 2004-07-29 | Macrogenics, Inc. | IDENTIFICATION AND ENGINEERING OF ANTIBODIES WITH VARIANT Fc REGIONS AND METHODS OF USING SAME |
WO2004063355A2 (en) | 2003-01-10 | 2004-07-29 | Protein Design Labs, Inc. | Novel methods of diagnosis of metastatic cancer, compositions and methods of screening for modulators of matastatic cancer |
EP2003196A3 (en) | 2003-06-09 | 2009-01-07 | The Regents of the University of Michigan | Compositions and methods for treating and diagnosing cancer |
WO2005032495A2 (en) | 2003-10-03 | 2005-04-14 | Bayer Pharmaceuticals Corporation | Gene expression profiles and methods of use |
DE10354601B3 (de) | 2003-11-21 | 2005-06-23 | Chiropro Gmbh | Gelenkprothese für Fingerglieder |
WO2005052182A2 (en) | 2003-11-26 | 2005-06-09 | Yissum Research Development Company Of The Hebrew University Of Jerusalem | A method of analyzing plasma membrane protein content of cells |
US20080119412A1 (en) | 2003-12-23 | 2008-05-22 | Nono Inc. | Polypeptides for Modulating Binding of Trp Channel Proteins and Trp- Associated Proteins |
WO2005076939A2 (en) | 2004-02-09 | 2005-08-25 | University Of Kentucky Research Foundation | Assay and method for diagnosing and treating alzheimer’s disease |
AU2005216922A1 (en) | 2004-02-26 | 2005-09-09 | Icoria, Inc. | Diagnosis of hyperinsulinemia and type II diabetes and protection against same based on genes differentially expressed in muscle cells |
TW200539855A (en) * | 2004-03-15 | 2005-12-16 | Wyeth Corp | Calicheamicin conjugates |
US20050255041A1 (en) | 2004-05-13 | 2005-11-17 | Arius Research, Inc. | Cancerous disease modifying antibodies |
DE102004024617A1 (de) | 2004-05-18 | 2005-12-29 | Ganymed Pharmaceuticals Ag | Differentiell in Tumoren exprimierte Genprodukte und deren Verwendung |
EP2302394A1 (en) | 2004-05-21 | 2011-03-30 | The Institute for Systems Biology | Compositions and methods for quantification of serum glycoproteins |
WO2006023121A1 (en) | 2004-07-27 | 2006-03-02 | Ohio University | Diagnosis of hyperinsulinemia and type ii diabetes and protection against same based on genes differentially expressed in white adipose tissue (13) |
DE102004042822A1 (de) | 2004-08-31 | 2006-03-16 | Technische Universität Dresden | Verbindungen und Methoden zur Behandlung, Diagnose und Prognose bei Pankreaserkrankungen |
FR2876705B1 (fr) | 2004-10-19 | 2008-12-12 | Biomerieux Sa | Procede pour le diagnostic d'une intolerance a l'aspirine |
US20070072175A1 (en) | 2005-05-13 | 2007-03-29 | Biogen Idec Ma Inc. | Nucleotide array containing polynucleotide probes complementary to, or fragments of, cynomolgus monkey genes and the use thereof |
ATE549624T1 (de) | 2005-07-01 | 2012-03-15 | Arbor Vita Corp | Verfahren und zusammensetzungen zur diagnose und behandlung von grippe |
AU2006280321A1 (en) | 2005-08-15 | 2007-02-22 | Genentech, Inc. | Gene disruptions, compositions and methods relating thereto |
EP1929003A4 (en) | 2005-08-31 | 2009-04-29 | Cell Signaling Technology Inc | REAGENTS FOR DETECTION OF PROTEIN PHOSPORYLATION IN CARCINOMA SIGNALING PATHWAYS |
EP2402758B1 (en) | 2005-09-19 | 2014-09-10 | Janssen Diagnostics, LLC | Methods and uses for identifying the origin of a carcinoma of unknown primary origin |
US20070099251A1 (en) | 2005-10-17 | 2007-05-03 | Institute For Systems Biology | Tissue-and serum-derived glycoproteins and methods of their use |
EP1790664A1 (en) | 2005-11-24 | 2007-05-30 | Ganymed Pharmaceuticals AG | Monoclonal antibodies against claudin-18 for treatment of cancer |
WO2007115045A2 (en) | 2006-03-29 | 2007-10-11 | Genentech, Inc. | Diagnostics and treatments for tumors |
US20100129929A1 (en) | 2006-07-27 | 2010-05-27 | Roberto Polakewicz | Tyrosine Phosphorylation Sites |
CA2660286A1 (en) | 2006-08-09 | 2008-02-21 | Homestead Clinical Corporation | Organ-specific proteins and methods of their use |
WO2008021115A2 (en) | 2006-08-14 | 2008-02-21 | The Brigham And Women's Hospital, Inc. | Diagnostic tests using gene expression ratios |
WO2008082730A2 (en) | 2006-09-19 | 2008-07-10 | Novartis Ag | Biomarkers of target modulation, efficacy, diagnosis and/or prognosis for raf inhibitors |
CA2666185A1 (en) | 2006-10-11 | 2008-04-17 | Max-Planck-Gesellschaft Zur Forderung Der Wissenschaften E.V. | Influenza targets |
US20090018031A1 (en) | 2006-12-07 | 2009-01-15 | Switchgear Genomics | Transcriptional regulatory elements of biological pathways tools, and methods |
CA2671194A1 (en) | 2006-12-08 | 2008-06-19 | Asuragen, Inc. | Mir-20 regulated genes and pathways as targets for therapeutic intervention |
MX2009008307A (es) | 2007-02-01 | 2009-08-25 | Veridex Llc | Metodos y materiales para identificar el origen de un carcinoma de origen primario desconocido. |
EP1983002A3 (en) | 2007-04-19 | 2009-03-11 | Peter Hornbeck | Tyrosine phosphorylation sites and antibodies specific for them |
EP1997832A1 (en) | 2007-05-29 | 2008-12-03 | Ganymed Pharmaceuticals AG | Monoclonal antibodies against Claudin-18 for treatment of cancer |
CA2689974A1 (en) | 2007-06-08 | 2008-12-18 | Asuragen, Inc. | Mir-34 regulated genes and pathways as targets for therapeutic intervention |
WO2008152822A1 (ja) | 2007-06-15 | 2008-12-18 | Medinet Co., Ltd. | 医薬 |
US20100292303A1 (en) | 2007-07-20 | 2010-11-18 | Birrer Michael J | Gene expression profile for predicting ovarian cancer patient survival |
WO2009035497A2 (en) | 2007-08-08 | 2009-03-19 | Savidge Tor C | Disease related cysteine modifications and uses thereof |
EP2036987A1 (en) | 2007-09-17 | 2009-03-18 | Siemens Healthcare Diagnostics GmbH | Molecular markers for tumor cell content in tissue samples |
AU2008301694B2 (en) | 2007-09-19 | 2013-07-18 | Suntory Holdings Limited | Compositions Containing Sesamin-Class Compound(s) and Arachidonic Acid Class Compound(s) |
AU2008309520A1 (en) | 2007-10-12 | 2009-04-16 | The Provost, Fellows And Scholars Of The College Of The Holy And Undivided Trinity Of Queen Elizabeth, Near Dublin | Method for opening tight junctions |
WO2009102367A2 (en) | 2007-11-19 | 2009-08-20 | The Regents Of The University Of Colorado | Tight junction protein modulators and uses thereof |
WO2009148593A1 (en) | 2008-06-02 | 2009-12-10 | Nsabp Foundation, Inc. | Identification and use of prognostic and predictive markers in cancer treatment |
WO2010046889A1 (en) | 2008-10-23 | 2010-04-29 | Quark Pharmaceuticals, Inc. | Methods for delivery of sirna to bone marrow cells and uses thereof |
CN101381524A (zh) | 2008-10-24 | 2009-03-11 | 南开大学 | 单层氧化石墨与水溶性高分子增强复合材料 |
GB0904957D0 (en) | 2009-03-23 | 2009-05-06 | Univ Erasmus Medical Ct | Tumour gene profile |
WO2010120526A2 (en) | 2009-03-31 | 2010-10-21 | Emory University | Methods and systems for screening for and diagnosing dna methylation associated with autism spectrum disorders |
CN101584860A (zh) | 2009-04-27 | 2009-11-25 | 西安杰诺瓦生物科技有限公司 | 重组人Claudin18.2肿瘤疫苗及其制备方法 |
WO2010141093A2 (en) | 2009-06-04 | 2010-12-09 | The University Of Maryland, Baltimore | Co-signaling methods for treating cancers |
WO2011038461A1 (en) | 2009-10-01 | 2011-04-07 | Chipdx Llc | System and method for classification of patients |
AU2010326066A1 (en) | 2009-12-01 | 2012-06-21 | Compendia Bioscience, Inc. | Classification of cancers |
EP2366709A1 (en) | 2010-03-16 | 2011-09-21 | BioNTech AG | Tumor vaccination involving a humoral immune response against self-proteins |
JP6199036B2 (ja) | 2010-03-16 | 2017-09-20 | バイオエヌテック アーゲーBioNTech AG | 自己タンパク質に対する体液性免疫応答に関わる腫瘍ワクチン接種 |
US8945847B2 (en) | 2010-05-24 | 2015-02-03 | Yissum Research Development Company Of The Hebrew University Of Jerusalem Ltd. | Methods and kits for ascertaining biosafety of an agent |
CA2801107A1 (en) | 2010-06-07 | 2011-12-15 | F. Hoffman-La Roche Ag | Gene expression markers for predicting response to interleukin-6 receptor-inhibiting monoclonal antibody drug treatment |
US8454385B2 (en) | 2010-06-22 | 2013-06-04 | John Mezzalingua Associates, LLC | Coaxial cable connector with strain relief clamp |
US20130157891A1 (en) | 2010-06-24 | 2013-06-20 | Xiao-Jun Li | Organ specific diagnostic panels and methods for identification of organ specific panel proteins |
WO2012070014A2 (en) | 2010-11-26 | 2012-05-31 | Yissum Research Development Company Of The Hebrew University Of Jerusalem Ltd. | Identification of novel cell surface markers for pancreatic progenitor cells and definite endodermal cells |
JP5319023B2 (ja) | 2011-01-12 | 2013-10-16 | 森永乳業株式会社 | 免疫調節作用を有する乳を産生する食餌のスクリーニング法 |
DE102011005235B4 (de) | 2011-03-08 | 2017-05-24 | Sirs-Lab Gmbh | Verfahren zum Identifizieren einer Teilmenge von Polynucleotiden aus einer dem Humangenom entsprechenden Ausgangsmenge von Polynucleotiden zur in vitro Bestimmung eines Schweregrads der Wirtsantwort eines Patienten |
JP2015513913A (ja) | 2012-04-02 | 2015-05-18 | モデルナ セラピューティクス インコーポレイテッドModerna Therapeutics,Inc. | 修飾ポリヌクレオチド |
WO2013167153A1 (en) | 2012-05-09 | 2013-11-14 | Ganymed Pharmaceuticals Ag | Antibodies useful in cancer diagnosis |
WO2013174404A1 (en) | 2012-05-23 | 2013-11-28 | Ganymed Pharmaceuticals Ag | Combination therapy involving antibodies against claudin 18.2 for treatment of cancer |
WO2013174403A1 (en) | 2012-05-23 | 2013-11-28 | Ganymed Pharmaceuticals Ag | Combination therapy involving antibodies against claudin 18.2 for treatment of cancer |
WO2014025199A2 (ko) | 2012-08-09 | 2014-02-13 | 주식회사 한독 | 스테필로코칼 엔테로톡신 유래의 초항원 변이체 및 이에 표적 특이적 폴리펩타이드가 연결된 융합단백질 및 그 용도 |
WO2014025198A2 (ko) | 2012-08-09 | 2014-02-13 | 주식회사 한독 | Lfa3 변이체 및 상기 변이체 또는 lfa3 cd2 결합영역과 이에 표적 특이적 폴리펩타이드가 연결된 융합단백질 및 그 용도 |
WO2014031859A2 (en) | 2012-08-24 | 2014-02-27 | University Of Utah Research Foundation | Compositions and methods relating to blood-based biomarkers of breast cancer |
US20140073524A1 (en) | 2012-09-07 | 2014-03-13 | Institute For Systems Biology | Markers and methods for detecting posttraumatic stress disorder (ptsd) |
US9856532B2 (en) | 2012-09-07 | 2018-01-02 | Institute For Systems Biology | Markers and methods for detecting posttraumatic stress disorder (PTSD) |
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